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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013911Generated: October 27, 2026

2-Naphthalenethiol → HCID 178418688, compound

https://huagongshe.com/reaction/1013911

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphthalenethiolHCID 7058—
ReactantTriethylamineHCID 8471—
ReactantHCID 178418938HCID 178418938—
Solventtert-ButanolHCID 6386—
ProductHCID 178418688HCID 178418688—

Reaction Steps

To a solution of (5-cyclopropyl-2H-pyrazol-3-yl)-(2,6-dichloropyrimidin-4-yl)-amine (211 mg, 0.781 mmol) and 2-naphthalenethiol (125 mg, 0.781 mmol) in tert-butanol (5 mL) was added triethylamine (174 μL, 1.25 mmol) and the resulting mixture was heated at reflux for 15 hours. The reaction mixture was cooled to room temperature and partitioned between ethyl acetate and aqueous NaHCO3. The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, Hexane/AcOEt gradient) to afford [6-chloro-2-(naphthalen-2-ylsulfanyl)-pyrimidin-4-yl]-(5-cyclopropyl-2H-pyrazol-3-yl)-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982037B2
Source datasetuspto-grants-2011_07
ORD IDord-7a238266362748c89d93aac246e4d459
Source noteuspto-grants-2011_07